510(k) K934369 ยท KPN Alarm, Conditioned Response Enuresis
DRI SLEEPER
| Applicant | Laborie Medical Technologies, Ltd., Mississauga, CA |
| Decision | Substantially Equivalent, Nov 24, 1993 |
| Received | Sep 7, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K934369
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.